2013
DOI: 10.1186/2047-217x-2-4
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Ultra-deep sequencing enables high-fidelity recovery of biodiversity for bulk arthropod samples without PCR amplification

Abstract: BackgroundNext-generation-sequencing (NGS) technologies combined with a classic DNA barcoding approach have enabled fast and credible measurement for biodiversity of mixed environmental samples. However, the PCR amplification involved in nearly all existing NGS protocols inevitably introduces taxonomic biases. In the present study, we developed new Illumina pipelines without PCR amplifications to analyze terrestrial arthropod communities.ResultsMitochondrial enrichment directly followed by Illumina shotgun seq… Show more

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Cited by 239 publications
(296 citation statements)
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“…The potential for retrieving at least semiquantitative abundance data was confirmed for all markers, with 18S providing the strongest relationship between calanoid copepod biomass and number of HTS reads. However, alternatives to PCR‐based approaches may be required to accurately quantify species abundance with high‐throughput sequencing (Dowle, Pochon, Banks, Shearer, & Wood, 2015; Zhou et al., 2013). …”
Section: Resultsmentioning
confidence: 99%
“…The potential for retrieving at least semiquantitative abundance data was confirmed for all markers, with 18S providing the strongest relationship between calanoid copepod biomass and number of HTS reads. However, alternatives to PCR‐based approaches may be required to accurately quantify species abundance with high‐throughput sequencing (Dowle, Pochon, Banks, Shearer, & Wood, 2015; Zhou et al., 2013). …”
Section: Resultsmentioning
confidence: 99%
“…Enrichment of targeted molecules such as mitochondrial DNA may improve the problems associated with insufficient sequencing depth (Zhou et al 2013). Nonetheless, vast amounts of functional data produced in the metagenomics analyses promise a new paradigm in community ecology (Zhou et al 2015).…”
Section: Metagenomics Approachmentioning
confidence: 99%
“…Similarly to other amplicon-based methods, HTS techniques are sensitive to PCR and primer biases (Lindahl et al 2013). At least in theory, ultra-HTS technologies such as Illumina HiSeq may provide sufficient sequencing depth to detect barcode sequences from the entire metagenome as demonstrated for prokaryotes and soil animals (Zhou et al 2013;Logares et al 2014). The genomes of eukaryotes are typically several orders of magnitude larger compared to bacterial genomes such that the relative proportion of ribosomal DNA in the metagenome will be lower.…”
Section: Introductionmentioning
confidence: 99%
“…This finding is noteworthy because many ecological assessments work at the level of functional groups rather than at the level of species. Alternatively, PCR-free shotgun metagenomic approaches will be less prone to bias but require much higher sequencing depth (15), therefore increasing the cost for sufficient replication. Taxonomic coverage among animals will also increase with sequencing multiple independent markers [i.e., 18S, 16S (16)], but targeting nonprotein-coding genes may increase the probability of including sequencing artifacts.…”
Section: Va Flmentioning
confidence: 99%